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1.
Understanding the end state of black hole evaporation, the microscopic origin of black hole entropy, the information loss paradox, and the nature of the singularity arising in gravitational collapse - these are outstanding challenges for any candidate quantum theory of gravity. Recently, a midisuperspace model of quantum gravitational collapse has been solved using a lattice regularization scheme. It is shown that the mass of an eternal black hole follows the Bekenstein spectrum, and a related argument provides a fairly accurate estimate of the entropy. The solution also describes a quantized mass-energy distribution around a central black hole, which in the WKB approximation, is precisely Hawking radiation. The leading quantum gravitational correction makes the spectrum non-thermal, thus providing a plausible resolution of the information loss problem. 相似文献
2.
W. A. Rodrigues Jr. Q. A. G. de Souza J. Vaz Jr. P. Lounesto 《International Journal of Theoretical Physics》1996,35(9):1849-1900
In this paper we study Dirac-Hestenes spinor fields (DHSF) on a four-dimensional Riemann-Cartan spacetime (RCST). We prove that these fields must be defined as certain equivalence classes of even sections of the Clifford bundle (over the RCST), thereby being certain particular sections of a new bundle named the spin-Clifford bundle (SCB). The conditions for the existence of the SCB are studied and are shown to be equivalent to Geroch's theorem concerning the existence of spinor structures in a Lorentzian spacetime. We introduce also the covariant and algebraic Dirac spinor fields and compare these with DHSF, showing that all three kinds of spinor fields contain the same mathematical and physical information. We clarify also the notion of (Crumeyrolle's) amorphous spinors (Dirac-Kähler spinor fields are of this type), showing that they cannot be used to describe fermionic fields. We develop a rigorous theory for the covariant derivatives of Clifford fields (sections of the Clifford bundle, CB) and of Dirac-Hestenes spinor fields. We show how to generalize the original Dirac-Hestenes equation in Minkowski spacetime for the case of RCST. Our results are obtained from a variational principle formulated through the multiform derivative approach to Lagrangian field theory in the Clifford bundle. 相似文献
3.
Maria de Fátima V. Marques Danielle Ramos Juliana D. Rego 《European Polymer Journal》2004,40(11):2583-2589
Ethylene and different amounts of 1,7-octadiene were copolymerized using the metallocene catalyst system ethylidene-bis(fluorenyl) zirconium dichloride and methylaluminoxane (MAO) at both 50 and 90 °C. The catalyst activity has slightly increased with the addition of low amounts of the diene in relation to the homopolymerization of ethylene. The obtained polymers were characterized according to their melting temperature (Tm) and crystallinity degree (xc) by differential scanning calorimetry (DSC). Weight-average molecular weight (Mw) and polydispersity were determined by gel permeation chromatography (GPC). Diene contents in the copolymer were obtained through the FTIR spectroscopy. The results indicated that at polymerization temperature of 90 °C, crosslinking bonds in the obtained copolymers were low, differently from what was observed at 50 °C. The diene content in the copolymer achieved more than 3 mol% and the comonomer conversion was around 15%. Moreover, the obtained copolymers have Mw around 100,000 and large polydispersity. 相似文献
4.
Polysaccharide differences between planktonic and biofilm-associated EPS from Pseudomonas fluorescens B52 总被引:2,自引:0,他引:2
The polysaccharides associated with free (planktonic) and surface-attached (biofilm) cells from cultures of Pseudomonas fluorescens strain B52 were compared. Variations in the attached matrix due to surface material (glass or stainless steel) were also analyzed. Two digestion methods were used to optimize the recoveries of sugars, uronic acids and acidic substituents. The yield of analyzable material after digestion reached 90% for the material associated to the biofilms, though only 20–30% for that bound to planktonic cells. The polysaccharide(s) in the biofilm had glucuronic and guluronic acids as main components, besides rhamnose, glucose and glucosamine. The proportion of glucuronic to guluronic acid was higher in the polysaccharide(s) found in biofilms formed on stainless steel than in those on glass. 相似文献
5.
The kinetics of the oxidation of five catecholamines viz., dopamine (A), L-dopa (B), methyldopa (C), epinephrine (D) and norepinephrine
(E) by sodium N-chloro-p-toluenesulfonamide or chloramine-T (CAT) in presence of HClO4 was studied at 30±0.1 °C. The five reactions followed identical kinetics with a first-order dependence on [CAT]
o
, fractional-order in [substrate]
o
, and inverse fractional-order in [H+]. Under comparable experimental conditions, the rate of oxidation of catecholamines increases in the order D>E>A>B>C. The
variation of ionic strength of the medium and the addition of p-toluenesulfonamide or halide ions had no significant effect
on the reaction rate. The rate increased with decreasing dielectric constant of the medium. The solvent isotope effect was
studied using D2O. A Michaelis-Menten type mechanism has been suggested to explain the results. Equilibrium and decomposition constants for
CAT-catecholamine complexes have been evaluated. CH3C6H4SO2NHCl of the oxidant has been postulated as the reactive oxidizing species and oxidation products were identified. An isokinetic
relationship is observed with β=361 K, indicating that enthalpy factors control the reaction rate. The mechanism proposed
and the derived rate law are consistent with the observed kinetics. 相似文献
6.
The total synthesis of 1-(Z)-atractylodinol, a natural polyacetylenic alcohol with several biological activities, has been achieved using a newly developed telluride synthon and a novel use for the Negishi type coupling reaction employing vinyl tellurides. 相似文献
7.
Calorimetric measurements of the enthalpy of solution of cesium chromate gave ΔHsoln = (7622 ± 24) calth mol?1 for a dilution of Cs2CrO4·21128H2O. This result, along with the enthalpy of dilution gave the standard enthalpy of solution, ΔHsolno = (7512 ± 31) calth mol?1, whence the standard enthalpy of formation, ΔHf0(Cs2CrO4, c, 298.15 K), was calculated to be ?(341.78 ± 0.46) kcalth mol?1. Recomputed thermodynamic data for the formation of the other alkali metal chromates have been tabulated. From their solubilities and enthalpies of solution, the standard entropies, S0(298 K), of BaCrO4 and PbCrO4 were estimated to be (38.9 ± 0.9) and (43.7 ± 1.2) calth K?1 mol?1, respectively. There is evidence that ΔHf0(SrCrO4, c, 298.15 K) may be in error. Thermochemical, solubility, and equilibrium data, have been combined to update the thermodynamic properties of the aqueous chromate (CrO42?), bichromate (HCrO4?), and dichromate (Cr2O72?) ions. The new values at 298.15 K are as follows:
CrO42?(aq) | (13.8 ± 0.5) | ?(210.93 ± 0.45) | ?(174.8 ± 0.5) |
HCrO4?(aq) | (46.6 ± 1.8) | ?(210.0 ± 0.7) | ?(183.7 ± 0.5) |
Cr2O72?(aq) | (67.4 ± 3.9) | ?(356.5 ± 1.5) | ?(312.8 ± 1.0) |